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微小RNA-139通过靶向拓扑异构酶IIα抑制腔面型乳腺癌细胞的增殖。

MicroRNA-139 suppresses proliferation in luminal type breast cancer cells by targeting Topoisomerase II alpha.

作者信息

Hua Wei, Sa Ke-Di, Zhang Xiang, Jia Lin-Tao, Zhao Jing, Yang An-Gang, Zhang Rui, Fan Jing, Bian Ka

机构信息

Department of Obstetrics and Gynecology, Xijing Hospital, Fourth Military Medical University, Xi'an 710032, China; State Key Laboratory of Cancer Biology, Department of Biochemistry and Molecular Biology, Fourth Military Medical University, 710032 Xi'an, China.

State Key Laboratory of Cancer Biology, Department of Biochemistry and Molecular Biology, Fourth Military Medical University, 710032 Xi'an, China.

出版信息

Biochem Biophys Res Commun. 2015 Aug 7;463(4):1077-83. doi: 10.1016/j.bbrc.2015.06.061. Epub 2015 Jun 12.

Abstract

The classification of molecular subtypes of breast cancer improves the prognostic accuracy and therapeutic benefits in clinic. However, because of the complexity of breast cancer, more biomarkers and functional molecules need to be explored. Here, analyzing the data in a huge cohort of breast cancer patients, we found that Topoisomerase II alpha (TOP2a), an important target of chemotherapy is a biomarker for prognosis in luminal type breast cancer patients, but not in basal like or HER2 positive breast cancer patients. We identified that miR-139, a previous reported anti-metastatic microRNA targets 3'-untranslated region (3'UTR) of TOP2a mRNA. Further more, we revealed that the forced expression of miR-139 reduces the TOP2a expression at both mRNA and protein levels. And our functional experiments showed that the ectopic expression of miR-139 remarkably inhibits proliferation in luminal type breast cancer cells, while exogenous TOP2a expression could rescue inhibition of cell proliferation mediated by miR-139. Collectively, our present study demonstrates the miR-139-TOP2a regulatory axis is important for proliferation in luminal type breast cancer cells. This functional link may help us to further understand the specificity of subtypes of breast cancer and optimize the strategy of cancer treatment.

摘要

乳腺癌分子亚型的分类提高了临床预后准确性和治疗效果。然而,由于乳腺癌的复杂性,需要探索更多的生物标志物和功能分子。在此,通过分析大量乳腺癌患者的数据,我们发现拓扑异构酶IIα(TOP2a),一种化疗的重要靶点,是管腔型乳腺癌患者预后的生物标志物,但在基底样或HER2阳性乳腺癌患者中并非如此。我们确定,先前报道的具有抗转移作用的微小RNA miR-139靶向TOP2a mRNA的3'非翻译区(3'UTR)。此外,我们发现强制表达miR-139会在mRNA和蛋白质水平上降低TOP2a的表达。我们的功能实验表明,miR-139的异位表达显著抑制管腔型乳腺癌细胞的增殖,而外源性TOP2a的表达可以挽救miR-139介导的细胞增殖抑制。总体而言,我们目前的研究表明miR-139-TOP2a调控轴对管腔型乳腺癌细胞的增殖很重要。这种功能联系可能有助于我们进一步了解乳腺癌亚型的特异性并优化癌症治疗策略。

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